Investigating multi-leaf collimator tracking in stereotactic arrhythmic radioablation (STAR) treatments for atrial fibrillation

Suzanne Lydiard*, Vincent Caillet, Svenja Ipsen, Ricky O'Brien, Oliver Blanck, Per Rugaard Poulsen, Jeremy Booth, Paul Keall

*Corresponding author for this work

Abstract

Stereotactic arrhythmia radioablation (STAR) is an emerging treatment option for atrial fibrillation (AF). However, it faces possibly the most challenging motion compensation scenario: both respiratory and cardiac motion. Multi-leaf collimator (MLC) tracking is clinically used for lung cancer treatments but its capabilities with intracardiac targets is unknown. We report the first experimental results of MLC tracking for intracardiac targets. Five AF STAR plans of varying complexity were created. All delivered 5 × 10 Gy to both pulmonary vein antra. Three healthy human target motion trajectories were acquired with ultrasound and programmed into a motion platform. Plans were delivered with a linac to a dosimeter placed on the motion platform. For each motion trace, each plan was delivered with no MLC tracking and with MLC tracking with and without motion prediction. Dosimetric accuracy was assessed with γ-tests and dose metrics. MLC tracking improved the dosimetric accuracy in all measurements compared to non-tracking experiments. The average 2%/2 mm γ-failure rate was improved from 13.1% with no MLC tracking to 5.9% with MLC tracking (p < 0.001) and 7.2% with MLC tracking and no motion prediction (p < 0.001). MLC tracking significantly improved the consistency between planned and delivered target dose coverage. The 95% target coverage with the prescription dose (V100) was improved from 60% of deliveries with no MLC tracking to 80% of deliveries with MLC tracking (p = 0.03). MLC tracking was successfully implemented for the first time for intracardiac motion compensation. MLC tracking provided significant dosimetric accuracy improvements in AF STAR experiments, even with challenging cardiac and respiratory-induced target motion and complex treatment plans. These results warrant further investigation and optimisation of MLC tracking for intracardiac target motion compensation.

Original languageEnglish
Article number195008
JournalPhysics in Medicine and Biology
Volume63
Issue number19
ISSN0031-9155
DOIs
Publication statusPublished - 28.09.2018

Funding

The authors gratefully acknowledge funding from Australian Government NHMRC Program Grants APP1036078 and APP1132471 and the Australian Cancer Research Foundation.PJK is supported by an NHMRC Senior Principal Research Fellowship. The authors gratefully thank Ralf Bruder for his help with acquiring and processing the ultrasound target motion trajectories, Tobias Pommer for his contribution to the plan complexity analysis, Jung Kim for her assistance with the Hexamotion traces, and Helen Ball for her editing assistance. JB acknowledges the support of Scott Johnson and Varian Medical Systems for use of the Calypso system.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 9 - Industry, Innovation, and Infrastructure
    SDG 9 Industry, Innovation, and Infrastructure

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